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(Investigative Ophthalmology and Visual Science. 2004;45:2737-2746.)
© 2004 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.03-1047
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Temporal Changes in Gene Expression after Injury in the Rat Retina

Félix Vázquez-Chona, Bong K. Song, and Eldon E. Geisert, Jr

From the Department of Ophthalmology, University of Tennessee Health Science Center, Memphis, Tennessee.


   Abstract
Top
 Abstract
Methods
 Results
 Discussion
 References
 
PURPOSE. The goal of this study was to define the temporal changes in gene expression after retinal injury and to relate these changes to the inflammatory and reactive response. A specific emphasis was placed on the tetraspanin family of proteins and their relationship with markers of reactive gliosis.

METHODS. Retinal tears were induced in adult rats by scraping the retina with a needle. After different survival times (4 hours, and 1, 3, 7, and 30 days), the retinas were removed, and mRNA was isolated, prepared, and hybridized to the Affymatrix RG-U34A microarray (Santa Clara, CA). Microarray results were confirmed by using RT-PCR and correlation to protein levels was determined.

RESULTS. Of the 8750 genes analyzed, approximately 393 (4.5%) were differentially expressed. Clustering analysis revealed three major profiles: (1) The early response was characterized by the upregulation of transcription factors; (2) the delayed response included a high percentage of genes related to cell cycle and cell death; and (3) the late, sustained profile clustered a significant number of genes involved in retinal gliosis. The late, sustained cluster also contained the upregulated crystallin genes. The tetraspanins Cd9, Cd81, and Cd82 were also associated with the late, sustained response.

CONCLUSIONS. The use of microarray technology enables definition of complex genetic changes underlying distinct phases of the cellular response to retinal injury. The early response clusters genes associate with the transcriptional regulation of the wound-healing process and cell death. Most of the genes in the late, sustained response appear to be associated with reactive gliosis.

In response to local injury, the retina presents a characteristic series of changes at the site of injury. A secondary series of changes then spreads to involve the entire retina, often resulting in progressive degenerative changes and the formation of scar tissue.1 2 3 4 5 6 These responses of the retina to injury can be divided into an early acute phase, a delayed subacute phase, and a late chronic phase.1 4 6

The early phase, which occurs within the first few hours after injury, is characterized by hemorrhage,1 3 5 alterations in the glutamatergic system,7 changes in ionic balance,8 and the beginning of cell-death cascades.9 10 It is during this early phase that the first changes in the transcriptome occur, with upregulation of the immediate early genes.9 10 The retina then undergoes a series of delayed cellular responses that last for days. Among these responses is a generalized inflammatory reaction in which damaged cells release proinflammatory cytokines that recruit peripheral blood components.1 3 6 Many retinal cells experience cell-type–specific responses: dedifferentiation, degeneration, migration, hypertrophy, and proliferation.4 9 11 12 13 For example, Müller glial cells and the retinal pigmented epithelium (RPE) enter a reactive state in which they change protein expression, proliferate, and migrate into the wound and vitreous space.4 6 11 12 Inflammation and cell proliferation resolve within the first week as the response to injury enters its chronic phase.1 4 6 During the late phase, RPE and Müller cells remain reactive and participate in structural remodeling of the retina. Cells that migrate into the wound and vitreous space replace the hemorrhage with fibrocellular membranes.1 4 6 12 With time, these membranes may contract, causing significant problems, including retinal detachment.1 4 6 12

Progress in understanding the mechanisms controlling secondary injury has been significant. Gains have come about by focusing on individual molecules5 14 15 16 or groups of molecules7 8 9 17 and their participation in specific processes of the retinal healing response. However, many of the molecular events associated with activation of this response remain unknown. In the present study, we used microarray technology to catalog the expression of thousands of genes after retinal injury. Our first approach was discovery-driven, using the power of microarray to define the global patterns of gene expression changes. The second approach was hypothesis-driven, focusing on the role of Cd81 (whose product is involved in proliferation and gliosis15 16 18 19 20 ) and markers of reactive gliosis, including the cytoskeletal protein glial fibrillary acidic protein (GFAP).1 5 11 14 21 22


   Methods
Top
 Abstract
 Methods
Results
 Discussion
 References
 
Animals and Surgery
We used 59 male Sprague-Dawley (albino) rats (270–330 g) and 2 Long-Evans (pigmented) rats (350–400 g)—the latter in examining the response of the RPE to retinal injury (Table 1) . We anesthetized 47 albino rats and 2 pigmented rats by intraperitoneal injection of a mixture of xylazine (13 mg/kg) and ketamine (87 mg/kg), then induced a retinal tear in both eyes of each rat. For this purpose, we used a 27-gauge needle to penetrate the pars plana, then scraped the superior temporal retina medially to laterally, as previously described.15 16 21 22 Care was taken to prevent lens and sclera damage. Twelve control animals received no injury. All animals were killed by intraperitoneal injection of a mixture of xylazine (26 mg/kg) and ketamine (174 mg/kg). All protocols used in this study were approved by the Animal Care and Use Committee of the University of Tennessee Health Science Center and were in accordance with the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research.


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  		TABLE 1. Experiments and Distribution of Animals

 
Microarray Expression Profiles
Arrays, Sample Preparation, and Hybridization.
Using the rat RG-U34A oligonucleotide array (Affymetrix, Santa Clara, CA), we examined gene expression levels in the normal rat retina and injured rat retinas with 4-hour and 1-, 3-, 7-, and 30-day survival time (Table 1) . Retinas used for expression studies were dissected and examined under a stereomicroscope (model SXZ12; Olympus, Tokyo, Japan) and immediately processed. Nissl-stained sections of the eyecups showed that our retinal dissections included both the neural retina and RPE. We collected retinas from 36 animals—6 animals per experimental condition. For each experimental condition, we processed three independent retinal samples with two animals per sample. Thus, we collected 18 biological replicates and performed 18 hybridizations (Supplemental Table 1 at www.iovs.org/cgi/content/full/45/8/2737/DC1). We performed total RNA extraction (TRIzol; Invitrogen, Carlsbad, CA) and confirmed the integrity of RNA with a bioanalyzer (model 2100; Agilent Technologies, Palo Alto, CA). We synthesized, labeled, and hybridized cRNA onto arrays at Genome Explorations (Memphis, TN) according to standard Affymetrix methods, previously described by Rogojina et al.23

Data Extraction and Normalization.
We measured gene expression levels on computer (Microarray Suite 5.0; MAS 5.0; Affymetrix) and robust multiarray average (RMA)24 algorithms. Signals were log transformed (base 2), and the mean intensity for each microarray was normalized to 8 (log2 scale).23

Statistical and Clustering Analyses.
We determined the statistical significance of expression changes using Student’s t-test statistics. To determine the expected proportion of significant false positives, we used the false-discovery rate of Benjamini and Hochberg.25 Significantly expressed genes were clustered with CLUSFAVOR 6.0,26 using principal component analysis (PCA). Averages are expressed mean ± SEM.

MIAME Compliance and Availability of Microarray Data.
For further discussion on experimental design and other details of methods (MIAME report), see the online Appendix at www.iovs.org/cgi/content/full/45/8/2737/DC1. The raw MAS 5.0 data set is publicly available at Gene Expression Omnibus (www.ncbi.nlm.nih.gov/geo/ provided by the National Institute of Health, Bethesda, MD) as the group series GSE1001 (for individual accession numbers, see Supplemental Table 1).

One-Step RT-PCR
Using fluorescent, one-step reverse transcription-polymerase chain reaction (RT-PCR), we verified microarray expression changes for the early-response genes Fos and Fosl1, delayed-response genes Il1b and Irf1, and late-sustained response genes Cryab, Crygd, Cd81, and Gfap (nucleotide sequences shown in Supplemental Table 2 at www.iovs.org/cgi/content/full/45/8/2737/DC1). We performed primer design, one-step RT-PCR reaction, and RT-PCR analysis as previously described by Rogojina et al.23 To eliminate genomic contamination, we treated total RNA with RQ1 RNase-free DNase (Promega, Madison, WI). We performed RT-PCR reactions in a thermocycler (iCycler; Bio-Rad, Richmond, CA, using the reagents in the SYBR Green RT-PCR kit; Applied BioSystems, Warrington, UK). To determine the relative change in gene expression, we used the system software to compare the number of cycles (Ct) needed to reach the midpoint of the linear phase. All observations were normalized to the housekeeping gene Rps18.

Protein Expression and Localization
To determine the levels of protein expression in normal retinas and those at 7 days after injury, we used rabbit polyclonal antibody against glial fibrillary acidic protein (GFAP; Thermo Shandon, Pittsburgh, PA), a mouse monoclonal antibody AMP1 that recognizes CD81,19 and rabbit polyclonal antibodies against crystallin-{alpha}, -ß, and -{gamma} (provided by Sam Zigler, National Institutes of Health). The secondary antibodies were peroxidase conjugated goat anti-rabbit IgG, and goat anti-mouse IgG (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA), all of which had minimal cross-reactivity with rat serum proteins. We compared protein expression in injured retinas to control retinas using a previously described immunoblot method.15 16 19

Indirect immunohistochemical methods were used to define the cellular localization of GFAP and crystallins in sections of normal and injured retinas. Injured rats had survival times of 1, 3, 7, and 30 days after retinal injury (Table 1) . We anesthetized eight injured rats and three control rats, processed tissue, and followed immunohistochemical methods, as previously described.15 16 19 For fluorescence microscopy, we used fluorescein-conjugated donkey anti-rabbit IgG (Jackson ImmunoResearch Laboratories, Inc.). To identify RPE cells, we used a rhodamine-conjugated lectin from Phaseolus vulgaris (PHA-E; Sigma-Aldrich, St. Louis, MO), and mouse monoclonal anti-cytokeratin antibodies (CBL 234 and MAB 3412; Chemicon, Temecula, CA). We labeled nuclei with a fluorescent Nissl counterstain, Hoechst 33342 (Sigma-Aldrich), and examined the sections with a confocal laser scanning microscope (MRC-1024; Bio-Rad).


   Results
Top
 Abstract
 Methods
 Results
Discussion
 References
 
Glial and RPE Response to Retinal Injury
To characterize the local and global response to retinal injury, we examined the distribution of retinal glia and RPE cell markers. In normal retinas, anti-GFAP labeled astrocytes and Müller cell end feet in the ganglion cell layer (GCL; Fig. 1A ). PHA-E lectin stained the normal RPE, choroid, and outer segments (Fig. 1B , OS)—a pattern similarly described by Cho et al.27 After injury, the local response involved glia and RPE cells. As early as 3 days after injury, cells invading the retinal tear were labeled with anti-GFAP (Fig. 1D , arrow) or PHA-E lectin (Fig. 1E , arrow). Levels of GFAP and PHA-E labeling continued to increase so that by 30 days after injury, two cellular responses were observed at the site of injury. In one response, the cells filling the tear (Fig. 1I) , arrowheads) were mainly GFAP-positive glia cells (Fig. 1H , arrowheads). In the second response, RPE cells mainly filled the tear (Fig. 1K 1L , arrows) and glia cells formed a well-defined membrane separating the scar from the neural retina (Fig. 1J) . RPE cell response after retinal injury was consistent with the distribution of pigmented cells in injured Long-Evans rats (data not shown). In some instances, epiretinal membranes with glia (Fig. 1G , arrow) and RPE cells (Fig. 1H , arrow) formed projecting into the vitreous. Thus, local response to retinal injury involved glia and RPE cells in a manner consistent with previous studies.16 28



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  		FIGURE 1. The responses of the rat retina to injury. Retinas labeled with anti-glial fibrillary acidic protein (GFAP; A, D, G, J), lectin from Phaseolus vulgaris (PHA-E; B, E, H, K), and Hoechst nuclear staining (C, F, I, L). Shown are four regions of retina: normal (A– C), 3 days after injury (D– F), and two different retinas 30 days after injury (G– I, J– L). In normal retinas, anti-GFAP labeled astrocytes and Müller cell end feet at the GCL (A). PHA-E lectin stained the normal RPE, choroid, and outer segments (OS, B). At 3 days after injury, cells invading the retinal tear (F, arrow) labeled with anti-GFAP (D, arrow) or PHA-E lectin (E, arrow); whereas, near the injury anti-GFAP labeled mainly Müller cells and astrocytes at the GCL (D). At 30 days after injury, two cellular responses were observed at the site of injury. In one response, the cells filling the tear (I, arrows) were mainly glia cells (H, arrowheads). In the second response, RPE cells mainly filled the tear (K and L, arrows). In some instances, epiretinal membranes with glia (G, arrow) and RPE cells (H, arrow) formed over the retinal surface. A– C are of the same magnification and (D– L) are of the same magnification. Scale bar: (A, L) 50 µm.

 


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  		FIGURE 2. Differentially expressed genes (n = 194) were clustered into three major profiles: (A) an early response, (B) a delayed response, and (C) a late, sustained response. Genes were clustered using principal component analysis. Early-response genes displayed a transient surge in expression after injury. Genes fitting the delayed-response profile had a transient peak in expression at either 1 or 3 days after injury. Genes within the third expression profile had a late expression peak (i.e., at either 3 or 7 days) and sustained overexpression at 30 days after retinal injury. A complete list of upregulated genes organized by clusters is found online in Supplemental Table 3. The distribution of genes by functional category reveals that those within each expression profile are functionally related (D).

 
In addition to the local response, we observed the spread of GFAP immunoreactivity throughout the retina. During the first 3 days after injury, GFAP labeling was limited to Müller cells adjacent to the injury and to astrocytes in the GCL (Fig. 1D , arrow). At 7 and 30 days after injury, we observed a global GFAP labeling of the retina localized to astrocytes in the GCL, and to Müller cell processes (Fig. 1G 1J) . Near the site of injury, GFAP labeling showed that the Müller cell processes became thicker and extended into the subretinal space, whereas GFAP labeling of peripheral Müller cells extended from the GCL to the photoreceptor layer.

Microarray Expression Profiles
In our analysis of microarray data, we used two different tactics: a discovery-driven approach and a hypothesis-driven approach. In the discovery-driven approach, we defined different patterns of gene expression across the data set, clustering genes that might be functionally related. The hypothesis-driven approach focused on the gene expression of Cd81 and its relationship with reactive gliosis markers, particularly Gfap. This approach allowed us to concentrate on one aspect of the injury response to define the relationships within the tetraspanin family and markers of the reactive glial response.

Quality Controls.
The expression profiles (n = 18 arrays) met a strict set of quality-control parameters (Table 2) . Housekeeping genes displayed consistent values and 5' to 3' ratios of less than 3. The average percentage of Affymetrix-present calls across all arrays was 40.0% ± 1.1%. The intensity profiles (log2 scale) for all the arrays showed a normal distribution, with a mean at 6.59 ± 0.04 and an average SD ({sigma}2) of 2.32 ± 0.04. Comparison of expression profiles among arrays from independent replicates of the same experimental group (n = 3 arrays/group) showed a within-group average correlation of 0.92 ± 0.01. Our quality controls are consistent with published microarray data.10 29 30 Together, these results indicate integrity of starting RNA, and efficiency of first-strand cDNA synthesis and hybridization.


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  		TABLE 2. Microarray Expression Profiles in the Retina after an Experimentally-Induced Retinal Tear

 
Data Extraction and Normalization.
For temporal analysis of the data and comparison between data extraction methods, the mean intensity for each microarray was normalized to 8 (log2 scale). This transformation yielded MAS 5.0 signal intensities ranging from 1 to 18 relative units of fluorescence. To determine a "present" signal threshold in our system, we plotted the coefficient of variation versus the averaged signal value and determined the threshold signal yielding stable coefficients of variation. From this analysis, the present signal threshold was set at 8.64. Below this threshold, signals displayed coefficients of variation greater than 10%, whereas their variance increased exponentially (Supplemental Fig. 1 at www.iovs.org/cgi/content/full/45/8/2737/DC1). Using this criterion, 4480 (50.9%) of the genes met the present criterion in at least one condition and were considered for further analysis. We compared the present expression signals to RMA values and found an average correlation of 0.92 ± 0.01 (Supplemental Table 3 at www.iovs.org/cgi/content/full/45/8/2737/DC1).

To analyze further the reliability of our present signals, we compared multiples of change obtained with normalized MAS 5.0 and RMA to those obtained with RT-PCR (Table 3) . Using RT-PCR, we measured expression changes for Fos, Fosl1 (Fra-1), Il1b, Irf1, Cryab, Crygd, Cd81, and Gfap at 4 hours, 3 days, and 30 days after injury. For these genes, changes (x-fold) measured with normalized MAS 5.0, and RMA values were highly similar (r = 0.89). Both MAS 5.0 and RMA changes were similar in magnitude and direction to the changes obtained with RT-PCR. However, RT-PCR changes had higher correlations with normalized MAS 5.0 (r = 0.76) than with RMA (r = 0.58). Together, the high correlation between normalized MAS 5.0 values and RMA values and the similarity between microarray multiples of change and RT-PCR changes confirm the reliability of our present signals, which eliminate genes with low expression signals. Thus, we used the normalized MAS 5.0 data for our subsequent analysis.


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  		TABLE 3. Change Comparison among RT-PCR, MAS 5.0, and RMA

 
Discovery-Driven Analysis
The overall goal of our discovery-driven approach was to define groups of genes with similar expression patterns. The first step in the analysis defined 393 genes with significant changes in expression levels (change >1.7-fold and P < 0.02; Table 2 ). These differentially-expressed genes represented an average false discovery rate of 21.0% ± 5.1%. Collectively, these genes displayed a range of dynamic expression changes across survival time. The second step involved clustering the 393 genes into groups according to the similarity of their expression profiles. Using principal component analysis, we identified 194 upregulated genes having transcription changes that conformed to one of three major profiles: an early response (Fig. 2A) , a delayed response (Fig. 2B) , and a late, sustained response (Fig. 2C) . Early-response genes displayed a transient surge in expression after the retinal tear, whereas delayed response genes showed moderate upregulation at 4 hours and a delayed transient peak at either 1 or 3 days after injury. In contrast, late, sustained genes displayed peak upregulation at either 3 or 7 days and sustained overexpression at 30 days after injury. A complete list of upregulated genes organized by clusters is found in Supplemental Table 4 at www.iovs.org/cgi/content/full/45/8/2737/DC1.

The distribution of genes by functional category revealed that genes within clusters were functionally related (Fig. 2D) . For instance, 75% of the upregulated transcription genes clustered in the early-response profile. Additional functional groups represented in the early response included cell proliferation, apoptosis, and cell-survival mechanisms. Genes highly represented in the delayed-response profile included those regulating cell cycle, cell death, and survival, neural development, and gliosis. A high percentage of late, sustained genes were associated with the reactive responses of the retina: gliosis, inflammation, stress response, neuronal degeneration, and tissue remodeling. A summary and expanded version of the distribution of genes by clusters and functional category are shown in Figure 3 and Supplemental Table 5 (www.iovs.org/cgi/content/full/45/8/2737/DC1), respectively.



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  		FIGURE 3. Temporal distribution of genes and functional categories after retinal injury. Location of genes describes relative gene expression peaks: early expression corresponds to a peak expression at 4 hours, delayed expression corresponds to a peak expression at 1 or 3 days, and late expression corresponds to a peak expression at 7 or 30 days. For specific expression profiles, see Supplemental Table 4.

 
One unexpected finding in our analysis was the clustering of the crystallin genes with the retinal reactive marker Gfap. All the crystallins in the microarray—Cryaa, Cryab, Cryba1, Cryab4, Crybb2, Crybb3, Crygc, Crygd, and Cryge—displayed strong, sustained upregulation after the placement of retinal tears (Supplemental Table 5, category 7). To confirm our findings, we examined the mRNA and protein expression of selected crystallins. We measured the mRNA expression of Cryab and Crygd, using RT-PCR. Cryab mRNA levels showed a moderate increase of 1.42 ± 0.11-fold at 4 hours after injury, a robust upregulation of 4.13 ± 0.12-fold at 3 days, and a moderate change of 1.46 ± 0.04-fold at 30 days (Fig. 4A) . Crygd mRNA showed an initial downregulation of 1.34 ± 0.03-fold, followed by significant changes to 6.36 ± 0.25-fold at 3 days and 3.64 ± 0.41-fold at 30 days (Fig. 4A) . Our microarray and RT-PCR measurements showed agreement in the direction of change of Cryab and Crygd (Fig. 4A) . Moreover, the mRNA expression of Cryab and Crygd across time displayed a pattern of expression that was similar to that of genes in our late, sustained profile, with a delayed peak at 3 days and strong, sustained upregulation even after 30 days.



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  		FIGURE 4. Crystallin-{alpha}, -ß, and -{gamma} were dramatically upregulated after retinal injury. The microarray expression changes for Cryab and Crygd (A, ) were confirmed with RT-PCR (A, {square}). Immunoblots show increased levels of crystallin-{alpha}, -ß, and -{gamma} proteins (B). Crystallin-{alpha}, -ß, and -{gamma} expression in normal retinas (C, E, G, respectively) and injured retinas 7 days after injury (D, F, H, respectively) was localized by immunohistochemistry. In normal retina, crystallin immunoreactivity was present mainly in the GCL (C, E, G). Seven days after injury, there was a strong crystallin immunoreactivity throughout the scar spanning the retinal tear and protruded into the vitreous space (data not shown). High immunoreactivity levels for crystallin-{alpha} (D), -ß (F), and -{gamma} (H) were found immediately adjacent to the retina at GCL and outer segment layer (OS). No staining was seen when secondary antibody control was used (data not shown). (A) Significant changes from normal: t-test, *P < 0.05, **P < 0.01.

 
To extend our crystallin gene findings, we measured the protein levels of the crystallin-{alpha}, -ß, and -{gamma}, using a quantitative immunoblot method (Fig. 4B) . The immunoreactivity of each of these crystallins significantly increased to 7.1 ± 0.39-fold, 6.8 ± 0.66-fold, and 11.1 ± 2.4-fold, respectively, at 7 days after injury. Taking this analysis one step further, we defined the localization of the reactivity of crystallin-{alpha}, -ß, and -{gamma} in normal and injured retinas. In normal retinas, we observed labeling of these crystallins mainly in the GCL (Figs. 4C 4E 4G) . All three crystallins had well-defined patterns of immunoreactivity at the site of injury and within the layers of the retina. At 7 and 30 days after injury, immunoreactivity of these crystallins was seen throughout the scar that spanned the retinal tear and protruded into the vitreous space. Immediately adjacent to the injury, strong crystallin immunostaining was present in the GCL and the photoreceptor layer (Figs. 4D 4F 4H ; 7-day retinas shown). Moderate levels of immunoreactivity were also observed throughout the inner plexiform layer, the inner nuclear layer, and the RPE. The well-defined pattern of crystallin mRNA upregulation by microarray and RT-PCR as well as the increase of crystallin protein and crystallin localization in the retina by immunohistochemical methods validate our discovery-driven observations that crystallins displayed strong, sustained transcription in response to injury in the rat retina.

Hypothesis-Driven Approach
The primary interest of our laboratory is the role of CD81 in the healing response of the retina. We specifically examined the relationships between Cd81, other tetraspanins, and markers of reactive glia. Our microarray data showed that Cd81 was moderately upregulated at 4 hours, to 1.05 ± 0.1-fold, and significantly increased to 1.99 ± 0.2-fold and 1.88 ± 0.1-fold at 3 and 30 days, respectively (Fig. 5A , gray boxes). RT-PCR confirmed the sustained upregulation of Cd81 mRNA after retinal injury ((Fig. 5A) , white boxes). Our analysis showed that Cd81 clustered in the late, sustained profile, along with the tetraspanins and several glial reactive markers (see Supplemental Table 4, genes 126–194). We used a second round of PCA to define further the associations between Cd81 and the late, sustained profile genes. The subclusters were visualized by plotting the first two components (Fig. 5B) . Cd81 clustered tightly with tetraspanins Cd9 and Cd82, as well as with the genes for associated proteins major histocompatibility complex [MHC] class I (RT1Aw2 and RT1.Dau) and MHC class II (RT1.C/E). Together, these genes displayed persistent changes after retinal injury, with peak expression occurring at 3 days after injury. Tetraspanins Cd37, Cd53, and Cd151 were present in the normal retina, but their expression remained constant after injury. Among the glial reactive markers, Anxa5, Cntf, Pea15, Pmp22, S100a1, and Sparc clustered tightly with Cd81, whereas Clu, Cryab, Gfap, and A2m formed a separate cluster within the late sustained profile (Fig. 5B) .



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  		FIGURE 5. Cd81 clustered into the late-response profile along with tetraspanins and glial reactive markers. RT-PCR confirmed the sustained upregulation of Cd81 after injury (A). A second round of principal component analysis was used to define further the associations between Cd81 and the genes within the late-response profile. The subclusters were visualized by plotting the first two components (B). Cd81 clustered tightly with tetraspanins Cd9 and Cd82, as well as with the genes for associated proteins MHC class I (RT1Aw2 and RT1.Dau) and MHC class II (RT1.C/E). (A) Significant changes from normal: t-test, *P < 0.05, **P < 0.01.

 

   Discussion
Top
 Abstract
 Methods
 Results
 Discussion
References
 
The results of our microarray analysis describe both a local reactive response at the site of retinal injury and changes occurring across the entire retina. As with injuries in other parts of the central nervous system (CNS),31 a local glial response is identified by the dramatic upregulation of the cytoskeletal protein GFAP. In the retina, this occurs in both Müller cells and astrocytes.4 5 11 21 Reactive Müller glia cells hypertrophy, proliferate, and form a protective barrier around the damaged area.5 11 21 Studies done in our laboratory16 and by others5 21 have identified the spread of GFAP reactivity over the entire retina, even after a modest local insult. This global GFAP response has been observed in association with various types of injury, including retinal detachment,4 mechanical injury,15 16 21 22 laser lesions,5 and optic nerve injury,14 as well as after transplantation of retinal cells.6 Widespread spatial changes have also been reported for CD81,16 heat shock protein 27,32 clusterin,33 and NF-{kappa}B.17 34 Therefore, by examining changes over the entire retina, we measured in a consistent way the local and global response to the retinal tear.

The initial set of differentially expressed genes included 393 genes, 4.5% of the genes in the RG-U34A chip. Using clustering analysis,26 30 35 we discovered three major expression profiles: an early response, a delayed response, and a late, sustained response. Genes within each of the profiles were functionally related. The early-response profile reflects rapid transcription of the immediate early genes and genes involved in cell proliferation, apoptosis, and cell survival. Genes highly represented in the delayed profile included those with functions relating to the cell cycle, cell death and survival, neural development, and gliosis. Within the late, sustained profile, a high percentage of genes were associated with the reactive response of the retina: gliosis, inflammation, stress response, neuronal degeneration, and tissue remodeling. The clustering of functionally-related genes during retinal wound healing suggests that genes within a profile may be coregulated. Others35 36 have identified transcriptional networks controlling clusters of genes expressed during the cell-cycle progression in yeast Saccharomyces cerevisiae. Spellman et al.36 also found that genes in a given cluster share common regulatory motifs in the promoter region. Ongoing work in our laboratory reveals that selected genes within a cluster may be under the control of a common regulatory network (Geisert EE, et al. IOVS 2003;44:ARVO E-Abstract 2967).

The temporal regulation of genes and functional groups we observed is consistent with the results of previous studies of gene expression in the retina,9 10 brain,29 and spinal cord.30 For example, early gene expression of the transcription factors c-Fos, Fosl1 (Fra-1), Nfkb1, Stat3, Egr1 (Krox-24/NGFI-A), Cebpd, Atf3, and Irf1 has been reported in response to retinal ischemia,10 photopic injury,9 and retinal detachment.4 17 Moreover, the progression of gene expression changes in our study reflects the biochemical, cellular, and morphologic changes previously reported.1 4 5 7 8 9 10 11 12 13 17 An initial inflammatory response1 3 5 21 and change in ionic balance7 8 are followed by a series of cellular responses that include RPE and Müller cell reactivity and proliferation, and cell death.4 9 11 12 13 During the late response, the reactive RPE and Müller cells participate in structural remodeling of the retina, including the formation of fibrocellular membranes.1 4 6 12 Our results demonstrate that microarray clustering analysis can identify components of biochemical complexes and cellular pathways involved in the response of the retina to injury.

Given the importance of Müller cells, astrocytes, and microglia in the response of the retina to injury, genes associated with reactive gliosis are of particular interest. In this study, a significant group of gliosis-related genes clustered with Gfap in the late, sustained profile (Fig. 3) . Several of these gliosis-related factors, including Cp,37 ciliary neurotrophic factor (CNTF),38 apolipoprotein (Apo)E,39 CLU,33 Anxa5,10 S100,13 and secreted protein, acidic and rich in cysteine (SPARC),40 are known to be expressed by reactive Müller and RPE cells. Whereas mrf-1, Pea15, and Pmp22 genes were unexpectedly upregulated in the retina, although they are expressed by reactive glia elsewhere in the nervous system.41 42 43 Potential factors controlling glial activation in the retina include cytokines and inflammatory transcription factors. Cytokines and their receptors that are upregulated in our microarray data and are thought to play a key role in the modulation of glial cell function include IL-1ß, IL-6R, and CNTF.38 44 The actions of these cytokines in glia cells are mainly mediated by the transcription factors signal transducer and activator of transcription (STAT)-3 and NF-{kappa}B.44 For example, intravitreal injections of CNTF or IL-6 activate STAT3 in Müller cells.38 The reactive glia genes targeted by STAT3 include Gfap, A2m, Fos, Irf1, and Stat3.38 44 45 In addition, Müller cells show NF-{kappa}B activation within hours after retinal detachment.17 It is noteworthy that NF-{kappa}B also modulates the expression of Gfap as well as Il1b and Il6.44 Together, these data suggest that STAT3 and NF-{kappa}B mediate signaling pathways involved in the glial response to retinal injury.

One novel finding in our analysis was the profound upregulation of crystallin-{alpha}, -ß, and -{gamma} (Fig. 2) . Traditionally, crystallins have been thought to be lens-rich proteins involved in lens development and maintenance. However, recent studies10 46 47 48 49 50 suggest that crystallins have broader roles and are expressed beyond lens tissue. Gene-sequence homology studies of crystallins show that members of this family display considerable homology with genes involved in the stress response.46 47 For instance, the {alpha}-crystallins belong to the small heat-shock protein family and may act as molecular chaperones.46 47 In cultured RPE, {alpha}B-crystallin upregulation confers resistance to stress-inducible apoptosis.48 A recent gene expression study confirmed the increased expression of selected {alpha}, ß, and {gamma} crystallin transcripts in the rat retina after ischemia-reperfusion injury.10 Similarly, we found that the mRNA of all 10 crystallins represented in the microarray displayed strong, sustained upregulation after retinal injury. These results are consistent with the increased crystallin protein expression confirmed by Sakaguchi et al.49 using mass spectrometry after exposing rat retina to light injury. Furthermore, the temporal and spatial expression of crystallins is similar to that of GFAP, implicating this family of proteins in both the local and global response of the retina to trauma. Notably, studies of gene expression in the brain29 and spinal cord30 using the identical microarray platform (RG-U34A) did not find a similar upregulation in crystallin-{alpha}, -ß, and -{gamma} in response to trauma. Whereas crystallin expression in normal mouse retina displays animal-to-animal variation,50 studies after retinal detachment,10 light injury,49 and our retinal tear consistently report the upregulation of crystallins. The coordinated upregulation of crystallins after injury is a potentially important part of the retinal wound-healing process that merits further investigation. Defining the response of the crystallin family to injury illustrates the power of microarray technologies and the discovery-driven approach.

Microarray technology, combined with gene expression profiling, offers the potential to identify cellular pathways and molecular complexes that are essential to the regulation of retinal responses to trauma and disease.9 10 Our laboratory is defining the role of CD81 in reactive gliosis in the retina,15 16 brain,20 and spinal cord.18 CD81 is part of a molecular complex within the plane of the membrane that links adhesive interactions into second-messenger cascades.51 52 Using microarray technology, we monitored gene expression changes for Cd81 and the entire family of tetraspanins (e.g., Cd9, Cd37, Cd53, Cd63, Cd81, Cd82, and Cd151).51 52 In addition, we specifically mined the data to define changes in molecules known to associate with this family of proteins to determine whether the members of the tetraspanin complex are coregulated. Our analysis indicates that similar patterns of expression are shared by the tetraspanin genes Cd9, Cd81, and Cd82, as well as genes for the MHC receptors RT1Aw2, RT1.Dau, and RT1.C/E (Fig. 3) . Tetraspanins CD81, CD9, and CD82 are known to associate with MHC receptors in a number of different cell types, including lymphocytes, endothelial cells, and oocytes.51 52 53 For instance, CD81 and CD82 interact with MHC class I and II in antigen-presenting cells to modulate signaling through MHC molecules and antigen presentation.53 Defining the temporal expression of the tetraspanins and the molecules to which they complex allows us to focus on the specific role of CD81 in the retina, its potential molecular associations, and its role in the reactive response.

The present study catalogued the time course of expression changes in response to a retinal injury. By surveying the expression patterns of 8750 genes, we defined an early, a delayed, and a late, sustained response to retinal injury and demonstrated that within each profile, genes participate as functional units involved in different aspects of the healing response. Within the late response profile, we identified a host of glial reactive genes as well as crystallins, a previously overlooked family of proteins in the injured retina. In profiling the expression of tetraspanins, we identified CD9, CD81, and CD82 as potential organizers of molecular complexes regulating proliferation and the glial activation response. Our finding that crystallins and tetraspanins can act in functional units highlights the fact that the function, or therapeutic intervention, of a gene can be regulated at the gene expression level. However, we are limited in our ability to link crystallins or tetraspanins to specific cell populations or specific pathways. Future research using single-cell studies and genetically altered animals will help dissect the molecular pathways and networks regulating gene expression.


   Acknowledgements
 
The authors thank Samuel Zigler at the National Eye Institute for the gift of the rabbit polyclonal antibodies against crystallins; Grace R. Geisert and William E. Orr for technical assistance; and Edward Chaum and David Twombly for valuable comments on the manuscript.


   Footnotes
 
Supported by National Eye Institute Grant R01EY12369 (EEG), Core Grant 5P30 E7013080-04S1, and by an unrestricted grant from Research to Prevent Blindness, Inc.

Submitted for publication September 23, 2003; revised February 4, 2004; accepted March 9, 2004.

Disclosure: F. Vázquez-Chona, None; B.K. Song, None; E.E. Geisert, Jr, None

The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C. §1734 solely to indicate this fact.

Corresponding author: Eldon E. Geisert, Jr, Department of Ophthalmology, University of Tennessee Health Science Center, 855 Monroe Avenue, Memphis, TN 38163; egeisert{at}utmem.edu.


   References
Top
 Abstract
 Methods
 Results
 Discussion
 References
 

  1. Ryan SJ, Stout JT, Dugel PV. Posterior penetrating ocular trauma. Ryan SJ eds. Retina. 1994;3:2235–2250. CV Mosby Co. St. Louis.
  2. Postel EA, Mieler WF. Posterior segment manifestations of blunt trauma. Guyer DR eds. Retina-Vitreous-Macula. 1999;1:831–843. WB Saunders Co. Philadelphia.
  3. Gregor Z, Ryan SJ. Combined posterior contusion and penetrating injury in the pig eye. II. Histological features. Br J Ophthalmol. 1982;66:799–804.[Abstract/Free Full Text]
  4. Fisher SK, Stone J, Rex TS, Linberg KA, Lewis GP. Experimental retinal detachment: a paradigm for understanding the effects of induced photoreceptor degeneration. Prog Brain Res. 2001;131:679–698.[Medline][Order article via Infotrieve]
  5. Humphrey MF, Constable IJ, Chu Y, Wiffen S. A quantitative study of the lateral spread of Müller cell responses to retinal lesions in the rabbit. J Comp Neurol. 1993;334:545–558.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  6. Behar-Cohen FF, Thillaye-Goldenberg B, de Bizemont T, et al. EIU in the rat promotes the potential of syngeneic retinal cells injected into the vitreous cavity to induce PVR. Invest Ophthalmol Vis Sci. 2000;41:3915–3924.[Abstract/Free Full Text]
  7. Sherry DM, Townes-Anderson E. Rapid glutamatergic alterations in the neural retina induced by retinal detachment. Invest Ophthalmol Vis Sci. 2000;41:2779–2790.[Abstract/Free Full Text]
  8. Szabo ME, Droy-Lefaix MT, Doly M, Carre C, Braquet P. Ischemia and reperfusion-induced histologic changes in the rat retina: demonstration of a free radical-mediated mechanism. Invest Ophthalmol Vis Sci. 1991;32:1471–1478.[Abstract/Free Full Text]
  9. Grimm C, Wenzel A, Hafezi F, Reme CE. Gene expression in the mouse retina: the effect of damaging light. Mol Vis. 2000;6:252–260.[Web of Science][Medline][Order article via Infotrieve]
  10. Yoshimura N, Kikuchi T, Kuroiwa S, Gaun S. Differential temporal and spatial expression of immediate early genes in retinal neurons after ischemia-reperfusion injury. Invest Ophthalmol Vis Sci. 2003;44:2211–2220.[Abstract/Free Full Text]
  11. Bringmann A, Reichenbach A. Role of Müller cells in retinal degenerations. Front Biosci. 2001;6:E72–E92.[Medline][Order article via Infotrieve]
  12. Grierson I, Hiscott P, Hogg P, Robey H, Mazure A, Larkin G. Development, repair and regeneration of the retinal pigment epithelium. Eye. 1994;8:255–262.
  13. Sahel JA, Albert DM, Lessell S, Adler H, McGee TL, Konrad-Rastegar J. Mitogenic effects of excitatory amino acids in the adult rat retina. J Exp Eye Res. 1991;53:657–664.
  14. Bignami A, Dahl D. The radial glia of Müller in the rat retina and their response to injury: an immunofluorescence study with antibodies to the glial fibrillary acidic (GFA) protein. Exp Eye Res. 1979;28:63–69.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  15. Clarke K, Geisert EE, Jr. The target of the antiproliferative antibody (TAPA) in the normal and injured rat retina. Mol Vision. 1998;4:3.[Medline][Order article via Infotrieve]
  16. Song BK, Geisert GR, Vazquez-Chona F, Geisert EE, Jr. Temporal regulation of CD81 following retinal injury in the rat. Neurosci Lett. 2003;338:29–32.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  17. Geller SF, Lewis GP, Fisher SK. FGFR1, signaling, and AP-1 expression after retinal detachment: reactive Müller and RPE cells. Invest Ophthalmol Vis Sci. 2001;42:1363–1369.[Abstract/Free Full Text]
  18. Dijkstra S, Geisert EE, Jr, Gispen WH, Bar PR, Joosten EA. Up-regulation of CD81 (target of the antiproliferative antibody; TAPA) by reactive microglia and astrocytes after spinal cord injury in the rat. J Comp Neurol. 2000;428:266–277.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  19. Geisert EE, Jr, Yang L, Irwin MH. Astrocyte growth, reactivity, and the target of the antiproliferative antibody, TAPA. J Neurosci. 1996;16:5478–5487.[Abstract/Free Full Text]
  20. Sullivan CD, Geisert EE, Jr. Expression of rat target of the antiproliferative antibody (TAPA) in the developing brain. J Comp Neurol. 1998;396:366–380.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  21. MacLaren RE. Development and role of retinal glia in regeneration of ganglion cells following injury. Br J Ophthalmol. 1996;80:458–464.[Abstract/Free Full Text]
  22. Miller NM, Oberdorfer M. Neuronal and neuroglial responses following retinal lesions in the neonatal rats. J Comp Neurol. 1981;202:493–504.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  23. Rogojina AT, Orr WE, Song BK, Geisert EE, Jr. Comparing the use Affymetrix to spotted oligonucleotide microarrays using two retinal pigment epithelium cell lines. Mol Vis. 2003;9:482–496.[Web of Science][Medline][Order article via Infotrieve]
  24. Irizarry RA, Bolstad BM, Collin F, Cope LM, Hobbs B, Speed TP. Summaries of Affymetrix GeneChip probe level data. Nucleic Acids Res. 2003;31:e15.[Abstract/Free Full Text]
  25. Reiner A, Yekutieli D, Benjamini Y. Identifying differentially expressed genes using false discovery rate controlling procedures. Bioinformatics. 2003;19:368–375.[Abstract/Free Full Text]
  26. Peterson LE. CLUSFAVOR 5.0 hierarchical cluster and principal component analysis of microarray-based transcriptional profiles. Genome Biol. 2002;3:SOFTWARE0002.[Medline][Order article via Infotrieve]
  27. Cho EY, Choi HL, Chan FL. Expression pattern of glycoconjugates in rat retina as analyzed by lectin histochemistry. Histochemical J. 2002;34:589–600.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  28. Liou GI, Pakalnis VA, Matragoon S, et al. HGF regulation of RPE proliferation in an IL-1B/retinal hole-induced rabbit model of PVR. Mol Vis. 2002;8:494–501.[Web of Science][Medline][Order article via Infotrieve]
  29. Matzilevich DA, Rall JM, Moore AN, Grill RJ, Dash PK. High-density microarray analysis of hippocampal gene expression following experimental brain injury. J Neurosci Res. 2002;67:646–663.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  30. Di Giovanni S, Knoblach SM, Brandoli C, Aden SA, Hoffman EP, Faden AI. Gene profiling in spinal cord injury shows role of cell cycle in neuronal death. Ann Neurol. 2003;53:454–468.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  31. Ridet JL, Malhotra SK, Privat A, Gage FH. Reactive astrocytes: cellular and molecular cues to biological function. Trends Neurosci. 1997;20:570–577.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  32. Strunnikova N, Baffi J, Gonzalez A, Silk W, Cousins SW, Csaky KG. Regulated heat shock protein 27 expression in human retinal pigment epithelium. Invest Ophthalmol Vis Sci. 2001;42:2130–2138.[Abstract/Free Full Text]
  33. Wong P, Ulyanova T, Organisciak DT, et al. Expression of multiple forms of clusterin during light-induced retinal degeneration. Curr Eye Res. 2001;23:157–165.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  34. Wu T, Chen Y, Chiang SK, Tso MO. NF-kappaB activation in light-induced retinal degeneration in a mouse model. Invest Ophthalmol Vis Sci. 2002;43:2834–2840.[Abstract/Free Full Text]
  35. Heyer LJ, Kruglyak S, Yooseph S. Exploring expression data: identification and analysis of coexpressed genes. Genome Res. 1999;9:1106–1115.[Abstract/Free Full Text]
  36. Spellman PT, Sherlock G, Zhang MQ, et al. Comprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization. Mol Biol Cell. 1998;9:3273–3297.[Abstract/Free Full Text]
  37. Chen L, Dentchev T, Wong R, et al. Increased expression of ceruloplasmin in the retina following photic injury. Mol Vis. 2003;30(9)151–158.
  38. Wang Y, Smith SB, Ogilvie JM, McCool DJ, Sarthy V. Ciliary neurotrophic factor induces glial fibrillary acidic protein in retinal Müller cells through the JAK/STAT signal transduction pathway. Curr Eye Res. 2002;24:305–312.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  39. Anderson DH, Ozaki S, Nealon M, et al. Local cellular sources of apolipoprotein E in the human retina and retinal pigmented epithelium: implications for the process of drusen formation. Am J Ophthalmol. 2001;131:767–781.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  40. Gilbert RE, Cox AJ, Kelly DJ, et al. Localization of secreted protein acidic and rich in cysteine (SPARC) expression in the rat eye. Connect Tissue Res. 1999;40:295–303.[Web of Science][Medline][Order article via Infotrieve]
  41. Tanaka S, Suzuki K, Watanabe M, Matsuda A, Tone S, Koike T. Upregulation of a new microglial gene, mrf-1, in response to programmed neuronal cell death and degeneration. J Neurosci. 1998;18:6358–6369.[Abstract/Free Full Text]
  42. Trencia A, Perfetti A, Cassese A, et al. Protein kinase B/Akt binds and phosphorylates PED/PEA-15, stabilizing its antiapoptotic action. Mol Cell Biol. 2003;23:4511–4521.[Abstract/Free Full Text]
  43. Atanasoski S, Scherer SS, Nave KA, Suter U. Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot-Marie-Tooth disease type 1A. J Neurosci Res. 2002;67:443–449.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  44. Acarin L, Gonzalez B, Castellano B. Glial activation in the immature rat brain: implication of inflammatory transcription factors and cytokine expression. Prog Brain Res. 2001;132:375–389.[Medline][Order article via Infotrieve]
  45. Horvath CM. STAT proteins and transcriptional responses to extracellular signals. Trends Biochem Sci. 2000;25:496–502.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  46. Horwitz J. Alpha-crystallin. Exp Eye Res. 2003;76:145–153.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  47. Piatigorsky J. Multifunctional lens crystallins and corneal enzymes: more than meets the eye. Ann N Y Acad Sci. 1998;842:7–15.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  48. Alge CS, Priglinger SG, Neubauer AS, et al. Retinal pigment epithelium is protected against apoptosis by alphaB-crystallin. Invest Ophthalmol Vis Sci. 2002;43:3575–3582.[Abstract/Free Full Text]
  49. Sakaguchi H, Miyagi M, Darrow RM, et al. Intense light exposure changes the crystallin content in retina. Exp Eye Res. 2003;76:131–133.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  50. Xi J, Farjo R, Yoshida S, Kern TS, Swaroop A, Andley UP. A comprehensive analysis of the expression of crystallins in mouse retina. Mol Vis. 2003;9:410–419.[Web of Science][Medline][Order article via Infotrieve]
  51. Boucheix C, Rubinstein E. Tetraspanins. Cell Mol Life Sci. 2001;58:1189–1205.[CrossRef][Web of Science][Medline][Order article via Infotrieve]
  52. Hemler ME. Specific tetraspanin functions. J Cell Bio. 2001;55:1103–1107.
  53. Szollosi J, Horejsi V, Bene L, Angelisova P, Damjanovich S. Supramolecular complexes of MHC class I, MHC class II, CD20, and tetraspan molecules (CD53, CD81, and CD82) at the surface of a B cell line JY. J Immunol. 1996;157:2939–2946.[Abstract]



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